Advances in cerebellar disorders: pre-clinical models, therapeutic targets, and challenges

被引:1
|
作者
Manto, Mario [1 ]
Cendelin, Jan [2 ]
Strupp, Michael [3 ,4 ]
Mitoma, Hiroshi [5 ]
机构
[1] Univ Mons, Serv Neurosci, Mons, Belgium
[2] Charles Univ Prague, Fac Med Pilsen, Dept Pathophysiol, Plzen, Czech Republic
[3] Ludwig Maximilians Univ Munchen, Dept Neurol, Munich, Germany
[4] Ludwig Maximilians Univ Munchen, German Ctr Vertigo & Balance Disorders, Munich, Germany
[5] Tokyo Med Univ, Dept Med Educ, Tokyo, Japan
关键词
Ataxia; cerebellum; DNA; metabolic; Purkinje; reserve; SCA; triplet; NEURAL STEM-CELLS; PICK TYPE-C; ACETYL-DL-LEUCINE; DOWNBEAT NYSTAGMUS; LYSOSOMAL STORAGE; EQUILIBRIUM BEHAVIOR; LURCHER MUTANT; MOUSE MODEL; NEUROTROPHIC FACTOR; DIFFERENTIAL ROLES;
D O I
10.1080/14728222.2023.2263911
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
IntroductionCerebellar ataxias (CAs) represent neurological disorders with multiple etiologies and a high phenotypic variability. Despite progress in the understanding of pathogenesis, few therapies are available so far. Closing the loop between preclinical studies and therapeutic trials is important, given the impact of CAs upon patients' health and the roles of the cerebellum in multiple domains. Because of a rapid advance in research on CAs, it is necessary to summarize the main findings and discuss future directions.Areas coveredWe focus our discussion on preclinical models, cerebellar reserve, the therapeutic management of CAs, and suitable surrogate markers. We searched Web of Science and PubMed using keywords relevant to cerebellar diseases, therapy, and preclinical models.Expert opinionThere are many symptomatic and/or disease-modifying therapeutic approaches under investigation. For therapy development, preclinical studies, standardization of disease evaluation, safety assessment, and demonstration of clinical improvements are essential. Stage of the disease and the level of the cerebellar reserve determine the goals of the therapy. Deficits in multiple categories and heterogeneity of CAs may require disease-, stage-, and symptom-specific therapies. More research is needed to clarify how therapies targeting the cerebellum influence both basal ganglia and the cerebral cortex, poorly explored domains in CAs.
引用
收藏
页码:965 / 987
页数:23
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